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临床试验/NL-OMON51678
NL-OMON51678招募中不适用

Repetitive Transcranial Magnetic Stimulation (rTMS) versus sham rTMS in Body Dysmorphic Disorder - rTMS-BDD

Academisch Medisch Centrum0 个研究点目标入组 56 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
56

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 64(—)

入选标准

  • 1. Age 18 to 65 years old;
  • 2. Diagnosed with Body Dysmorphic Disorder (BDD), based on Body Dysmorphic
  • Disorder - Yale Brown Obsessive Compulsive Scale (BDD-YBOCS);
  • 3. Nonresponse (defined as <50% response on symptoms measured by the BDD-YBOCS)
  • after one type of medication treatment, SSRI, maximum dose and adequate
  • 4. Medication is set 6 weeks prior to the start, and could not be changed
  • during the study

排除标准

  • Exclusion criteria
  • 1. Intracerebral metal implants (e.g. cochlear implant, brain stimulator);
  • 2. (History of) epilepsy or epilepsy in a first degree relative;
  • 3. Any other neurological disorder with seizure risk;
  • 4. Acute suicidal ideations, or any psychological crisis (contact with the
  • outpatient crisis service or admission in psychiatric hospital);
  • 5. Bipolar disorder;
  • 6. Current disorder in substance abuse (opiate, ketamine, LSD,
  • (meth)amphetamine, cocaine, solvents, cannabis, benzodiazepines or barbiturate)
  • or alcohol abuse;
  • 7. Any known other serious somatic health problem;
  • 8. Pregnancy;
  • 9. Primarily autism spectrum disorder or primarily personality disorder (using
  • SCID-5-P at baseline for personality disorders). Given that this is often seen
  • secondarily in BDD patients.
  • rTMS Contraindications:
  • 1. History of epileptic seizures or epilepsy in a first degree relative,
  • irregular sleep/ wake rhythm;
  • 2. Cardiac demand pacemakers;
  • 3. Implanted defibrillators;
  • 4. Implanted neurostimulators;
  • 5. Cochlear implants.

研究者

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